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In Brief: Defibrotide (Defitelio) for Hepatic Veno-Occlusive Disease
The Medical Letter on Drugs and Therapeutics • Sep 12, 2016 (Issue 1503)
properties that protect
hepatic endothelial cells from the damage associated
with HSCT.1
Approval ...
The FDA has approved defibrotide sodium (Defitelio – Jazz), a mixture of mostly single-stranded polydeoxyribonucleotide sodium salts, for treatment of adults and children with hepatic veno-occlusive disease (also known as sinusoidal obstruction syndrome) and renal or pulmonary dysfunction following hematopoietic stem cell transplantation (HSCT). It is the first drug to be approved by the FDA for treatment of severe hepatic veno-occlusive disease. Defibrotide was approved earlier by the European Medicines Agency for the same indication.Hepatic veno-occlusive disease is an uncommon (<2%)...
In Brief: New Benzodiazepine Warnings
The Medical Letter on Drugs and Therapeutics • Nov 02, 2020 (Issue 1610)
and physical dependence.1 Benzodiazepine
labels have contained a boxed warning about a risk of
serious drug ...
The FDA now requires boxed warnings in the package
inserts of benzodiazepines describing the potential for
these drugs to be abused and misused and to cause
addiction and physical dependence. Benzodiazepine
labels have contained a boxed warning about a risk of
serious drug interactions with opioids since 2016.
In Brief: A New Prostate Cancer Indication for Darolutamide (Nubeqa) (online only)
The Medical Letter on Drugs and Therapeutics • Jun 19, 2023 (Issue 1679)
of nonmetastatic castration-resistant
prostate cancer (nmCRPC).1
MECHANISM OF ACTION — Androgen receptors ...
The androgen receptor inhibitor darolutamide
(Nubeqa – Bayer) has been approved by the FDA
for use in combination with docetaxel for treatment
of metastatic hormone-sensitive prostate cancer
(mHSPC). The drug was previously approved for
treatment of nonmetastatic castration-resistant
prostate cancer (nmCRPC).
Med Lett Drugs Ther. 2023 Jun 19;65(1679):e108 doi:10.58347/tml.2023.1679h | Show Introduction Hide Introduction
In Brief: Melphalan (Hepzato) for Uveal Melanoma (online only)
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
duration of
response was 14 months.1 ADVERSE EFFECTS — In the FOCUS trial, cytopenias,
fatigue, nausea ...
...
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e148 doi:10.58347/tml.2023.1684d | Show Introduction Hide Introduction
Choice of Benzodiazepines
The Medical Letter on Drugs and Therapeutics • Feb 26, 1988 (Issue 760)
-qid 4.24
Valium (Roche) 12.38
Q-Pam (Quantum) 1.13
Lorazepam - average generic price intermediate ...
Since The Medical Letter last reviewed the choice of benzodiazepines (Volume 23, page 41, 1981), several new drugs have been marketed and some old ones are now available generically. Most of the benzodiazepines available for oral use in the USA are listed in the table on page 28.
Cefuroxime Axetil
The Medical Letter on Drugs and Therapeutics • Jun 03, 1988 (Issue 767)
elimination half-life is 1.2 hours. The major route of excretion is renal, by both glomerular
The Medical ...
Cefuroxime axetil (Ceftin - Glaxo), an oral form of the second-generation parenteral cephalosporin cefuroxime (Zinacef), was recently marketed in the USA. Previously available oral cephalosporins are the first-generation drugs cephalexin (Keflex; and others), cephradine (Anspor; and others) and cefadroxil (Duricef; and others), and the second-generation cefaclor (Ceclor); second-generation cephalosporins have more activity against gram-negative bacteria.
Cefixime - A New Oral Cephalosporin
The Medical Letter on Drugs and Therapeutics • Aug 11, 1989 (Issue 798)
for patients with renal impairment.
COST OF SOME ANTIMICROBIALS
Pediatric Adult
Drug Dosage
1
Cost
2 ...
Cefixime (Suprax - Lederle), an oral cephalosporin antibiotic, was recently approved for marketing by the US Food and Drug Administration. Claimed to be the first oral third-generation cephalosporin, the new drug is offered for once-a-day treatment of otitis media, pharyngitis, bronchitis and urinary tract infections.
Fluconazole
The Medical Letter on Drugs and Therapeutics • May 18, 1990 (Issue 818)
Saag and WE Dismukes, Antimicrob Agents Chemother, 32:1, 1988).
PHARMACOKINETICS — In comparison ...
Fluconazole (Diflucan - Roerig), an antifungal azole, was recently approved by the US Food and Drug Administration for oral and intravenous (IV) treatment of cryptococcal meningitis and various forms of candidiasis. Both cryptococcal meningitis and candidiasis occur frequently in patients with AIDS, organ transplants, or cancer.
Clozapine
The Medical Letter on Drugs and Therapeutics • Feb 19, 1993 (Issue 890)
reaction and a toxic metabolite have been implicated (SL Gerson and H Meltzer, Drug Safety, 7 suppl 1:17 ...
Clozapine (Clozaril - Sandoz), an antipsychotic drug, was first marketed in the USA three years ago (Medical Letter, 32:3, 1990). Because of its hematological toxicity, the US Food and Drug Administration approved the drug only for patients with schizophrenia who cannot tolerate or do not respond to standard antipsychotic drugs.
Carvedilol for Heart Failure
The Medical Letter on Drugs and Therapeutics • Sep 26, 1997 (Issue 1010)
sympathomimetic activity and is also an alpha
1
-blocker. In addition, the drug is a scavenger of oxygen
free ...
Carvedilol (Coreg - SmithKline Beecham and Boehringer-Mannheim), a betaadrenergic and alpha-adrenergic blocker approved by the FDA for treatment of hypertension in 1995, but not marketed at that time, has now been approved and marketed for treatment of mild or moderate (NYHA class II or III) heart failure stabilized on other drugs. It is being promoted as an add-on drug that reduces the morbidity and mortality of the disease.